Canonical Allele Identifier: CA369863862
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150959703G>T , CM000669.2:g.150959703G>T GRCh38
NC_000007.13:g.150656791G>T , CM000669.1:g.150656791G>T GRCh37
NC_000007.12:g.150287724G>T NCBI36
NG_008916.1:g.23224C>A , LRG_288:g.23224C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684241.1:n.1174C>A
ENST00000262186.10:c.341C>A MANE Select ENSP00000262186.5:p.Pro114His
ENST00000262186.9:c.341C>A ENSP00000262186.5:p.Pro114His
ENST00000430723.4:c.164C>A ENSP00000387657.4:p.Pro55His
ENST00000532957.5:n.564C>A
NM_000238.3:c.341C>A , LRG_288t1:c.341C>A NP_000229.1:p.Pro114His
NM_172056.2:c.341C>A , LRG_288t2:c.341C>A NP_742053.1:p.Pro114His
XM_011516185.1:c.41C>A XP_011514487.1:p.Pro14His
XM_011516186.1:c.341C>A XP_011514488.1:p.Pro114His
XM_011516185.2:c.41C>A XP_011514487.1:p.Pro14His
XM_011516186.3:c.341C>A XP_011514488.1:p.Pro114His
XM_017012195.1:c.191C>A XP_016867684.1:p.Pro64His
XM_017012196.1:c.164C>A XP_016867685.1:p.Pro55His
NM_000238.4:c.341C>A MANE Select NP_000229.1:p.Pro114His